PTPN22 1858 C/T Exon Polymorphism is not Associated with Graves' Disease in Kashmiri population

BACKGROUND: Graves' disease (GD) is a multifactorial autoimmune disease with contribution from both genetic and epigenetic factors in its causation. Association of genetic factors and GD has been extensively studied. Gene “protein tyrosine phosphatase nonreceptor 22” (PTPN22) is an important im...

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Detalles Bibliográficos
Autores principales: Shehjar, Faheem, Dil-Afroze, Misgar, Riaz A., Malik, Sajad A., Laway, Bashir A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085953/
https://www.ncbi.nlm.nih.gov/pubmed/30148088
http://dx.doi.org/10.4103/ijem.IJEM_105_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085953/
https://www.ncbi.nlm.nih.gov/pubmed/30148088
http://dx.doi.org/10.4103/ijem.IJEM_105_18

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